CDRH regulations
The Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration implemented regulations for laser products on August 2, 1976. Compliance is mandatory for products marketed in the United States. The label shown below indicates compliance with the CDRH regulations and must be attached to laser products marketed in the United States.
InterfacesParallel interfaceUse the IEEE
ECP mode/Nibble mode
USB interfaceUSB 2.0 High Speed mode
B B B B B B B B B B B B
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